Search Results - "Adkins, Elisabeth B"

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  1. 1

    Molecular identification of collagen 17a1 as a major genetic modifier of laminin gamma 2 mutation-induced junctional epidermolysis bullosa in mice by Sproule, Thomas J, Bubier, Jason A, Grandi, Fiorella C, Sun, Victor Z, Philip, Vivek M, McPhee, Caroline G, Adkins, Elisabeth B, Sundberg, John P, Roopenian, Derry C

    Published in PLoS genetics (01-02-2014)
    “…Epidermolysis Bullosa (EB) encompasses a spectrum of mechanobullous disorders caused by rare mutations that result in structural weakening of the skin and…”
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    Journal Article
  2. 2
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    The wooly mutation (wly) on mouse chromosome 11 is associated with a genetic defect in Fam83g by Radden, 2nd, Legairre A, Child, Kevin M, Adkins, Elisabeth B, Spacek, Damek V, Feliciano, Aaron M, King, Thomas R

    Published in BMC research notes (09-05-2013)
    “…Mice homozygous for the spontaneous wooly mutation (abbreviated wly) are recognized as early as 3-4 weeks of age by the rough or matted appearance of their…”
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    Journal Article
  4. 4

    Natural TFH arise in the thymus and periphery of young naive mice by Adkins, Elisabeth B, Wang, Xulong, Sproule, Thomas J, Christianson, Gregory G, Park, Giljun, Lane-Reiticker, Sarah-Kate, Jain, Shweta, Carter, Gregory W, Morse, Herbert C, Roopenian, Derry C

    Published in The Journal of immunology (1950) (01-05-2016)
    “…T follicular helper cells (TFH) localize to B cell follicles and secrete Interleukin 21 (IL21), a cytokine that is vital for driving the proliferation of…”
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    Journal Article
  5. 5

    The juvenile alopecia mutation (jal) maps to mouse Chromosome 2, and is an allele of GATA binding protein 3 (Gata3) by Ramirez, Francisco, Feliciano, Aaron M, Adkins, Elisabeth B, Child, Kevin M, Radden, 2nd, Legairre A, Salas, Alexis, Vila-Santana, Nelson, Horák, José M, Hughes, Samantha R, Spacek, Damek V, King, Thomas R

    Published in BMC genetics (09-05-2013)
    “…Mice homozygous for the juvenile alopecia mutation (jal) display patches of hair loss that appear as soon as hair develops in the neonatal period and persist…”
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    Journal Article
  6. 6

    Molecular Identification of Collagen 17a1 as a Major Genetic Modifier of Laminin Gamma 2 Mutation-Induced Junctional Epidermolysis Bullosa in Mice: e1004068 by Sproule, Thomas J, Bubier, Jason A, Grandi, Fiorella C, Sun, Victor Z, Philip, Vivek M, McPhee, Caroline G, Adkins, Elisabeth B, Sundberg, John P, Roopenian, Derry C

    Published in PLoS genetics (01-02-2014)
    “…Epidermolysis Bullosa (EB) encompasses a spectrum of mechanobullous disorders caused by rare mutations that result in structural weakening of the skin and…”
    Get full text
    Journal Article
  7. 7
  8. 8

    The juvenile alopecia mutation by Ramirez, Francisco, Feliciano, Aaron M, Adkins, Elisabeth B, Child, Kevin M, Radden II, Legairre A, Salas, Alexis, Vila-Santana, Nelson, Horák, Josñ M, Hughes, Samantha R, Spacek, Damek V, King, Thomas R

    Published in BMC genetics (09-05-2013)
    “…Mice homozygous for the juvenile alopecia mutation (jal) display patches of hair loss that appear as soon as hair develops in the neonatal period and persist…”
    Get full text
    Journal Article